Canonical Allele Identifier: CA429810474

Gene: CDCA7

Linked Data

• MyVariant Identifiers: chr2:g.174231055A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.173366327A>G , CM000664.2:g.173366327A>G	GRCh38
NC_000002.11:g.174231055A>G , CM000664.1:g.174231055A>G	GRCh37
NC_000002.10:g.173939301A>G	NCBI36
NG_047202.1:g.17311A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695901.1:c.798+735A>G	ENSP00000512251.1:n.798+735A>G
ENST00000695911.1:c.858A>G	ENSP00000512262.1:n.858A>G
ENST00000695912.1:c.1077A>G	ENSP00000512263.1:p.Lys359=
ENST00000695913.1:c.*1833A>G	ENSP00000512264.1:n.*1833A>G
ENST00000695914.1:c.840A>G	ENSP00000512265.1:p.Lys280=
ENST00000695918.1:n.308A>G
ENST00000306721.8:c.1080A>G MANE Select	ENSP00000306968.3:p.Lys360=
ENST00000306721.7:c.1080A>G	ENSP00000306968.3:p.Lys360=
ENST00000347703.7:c.843A>G	ENSP00000272789.4:p.Lys281=
ENST00000410019.3:c.717A>G	ENSP00000386833.3:p.Lys239=
ENST00000410101.7:c.948A>G	ENSP00000386656.3:p.Lys316=
ENST00000467411.5:n.1768+735A>G
ENST00000496441.5:n.1834A>G
NM_031942.4:c.1080A>G	NP_114148.3:p.Lys360=
NM_145810.2:c.843A>G	NP_665809.1:p.Lys281=
XM_011511957.1:c.999A>G	XP_011510259.1:p.Lys333=
XR_923034.1:n.1978A>G
NM_031942.5:c.1080A>G MANE Select	NP_114148.3:p.Lys360=
NM_145810.3:c.843A>G	NP_665809.1:p.Lys281=